SUNGLASSES— 510(k) K920344

Substantially Equivalent

J & D Products, Inc.

FDA 510(k) clearance K920344 for SUNGLASSES, Substantially Equivalent on 1992-04-21. Applicant: J & D Products, Inc.. Device class: 1.

Clearance details

Applicant: J & D Products, Inc.
Product code: Code HQY
Device class: Class 1
Regulation: 21 CFR 886.5850
Advisory panel: Ophthalmic
Date received: 1992-01-23
Decision date: 1992-04-21
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Jersey City, NJ, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code HQY

K974852 — NON-PRESCRIPTION SUNGLASSES1998-01-30
K974860 — NON-PRESCRIPTION SUNGLASSES1998-01-30
K974861 — NON-PRESCRIPTION SUNGLASSES1998-01-27
K974511 — SUNGLASSES1998-01-12
K974441 — SUNGLASSES1998-01-09

Data sourced from openFDA. This site is unofficial and independent of the FDA.